The Application of Hangman Fe(IV) Corrole in the Baeyer–Villiger Oxidation Reaction

Abstract A series of new hangman iron corroles with different electronic structure and pending aldehyde group were prepared and used as catalyst in Baeyer–Villiger (B–V) oxidation reactions. The results show that hangman iron corroles exhibit faster reaction rates and higher ε‐caprolactone yields as compared to triaryl iron 5,10,15‐tri(pentafluorophenyl) corrole (Fe(tpfc)Cl). With the increase in the electron‐withdrawing ability of the meso‐position substituents of hangman iron corrole, the yield of caprolactone also increases. Under optimal conditions, the best hangman iron corrole bearing two pentafluorophenyl groups (FePXC) may give a yield of 97% at only 0.07 mol% catalyst loading. The turnover number (TON) of the FePXC catalyst could be up to 2100 in a gram‐scale test of oxidation of cyclohexanone. This work demonstrates the good potential of hangman corroles in B–V oxidation.

Authors

Institutions

Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-06-07
DOI
https://doi.org/10.1002/ajoc.202500030
Primary Topic
Porphyrin and Phthalocyanine Chemistry
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

The Application of Hangman Fe(IV) Corrole in the Baeyer–Villiger Oxidation Reaction

Xinde Cao, Guo‐Chao Liang, Yi‐Feng Qiu, Hao Zhang et al.
1 links
Asian Journal of Organic Chemistry
Porphyrin and Phthalocyanine Chemistry
article

The Application of Hangman Fe(IV) Corrole in the Baeyer–Villiger Oxidation Reaction

Xinde Cao, Guo‐Chao Liang, Yi‐Feng Qiu, Hao Zhang, Haiyang Liu, Feng Li, Furong Wang
article en

Abstract

Abstract A series of new hangman iron corroles with different electronic structure and pending aldehyde group were prepared and used as catalyst in Baeyer–Villiger (B–V) oxidation reactions. The results show that hangman iron corroles exhibit faster reaction rates and higher ε‐caprolactone yields as compared to triaryl iron 5,10,15‐tri(pentafluorophenyl) corrole (Fe(tpfc)Cl). With the increase in the electron‐withdrawing ability of the meso‐position substituents of hangman iron corrole, the yield of caprolactone also increases. Under optimal conditions, the best hangman iron corrole bearing two pentafluorophenyl groups (FePXC) may give a yield of 97% at only 0.07 mol% catalyst loading. The turnover number (TON) of the FePXC catalyst could be up to 2100 in a gram‐scale test of oxidation of cyclohexanone. This work demonstrates the good potential of hangman corroles in B–V oxidation.

Asian Journal of Organic ChemistryVol. 14(8)
Wen's Food Group (China) (CN), South China University of Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 91%
Porphyrin and Phthalocyanine Chemistry
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

The Application of Hangman Fe(IV) Corrole in the Baeyer–Villiger Oxidation Reaction — Xinde Cao, Guo‐Chao Liang, et al. · Asian Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS